A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4622n54



Internal ID22772517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73368049..73368730hg38UCSC Ensembl
chr15:73660390..73661071hg19UCSC Ensembl
chr15:71447443..71448124hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38682
hg19682
hg18682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569965, nsv569963
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4622n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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